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Application of an HPLC method for analysis of propolis extract

dc.contributor.authorBruschi, M. L.
dc.contributor.authorFranco, S. L.
dc.contributor.authorGremiao, MPD
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:24:24Z
dc.date.available2014-05-20T13:24:24Z
dc.date.issued2003-01-01
dc.description.abstractPropolis obtained from honeybee hives has been widely used in medicine, cosmetics, and industry due to its versatile biological activities (antioxidant, antimicrobial, fungicidal, antiviral, antiulcer, immunostimulating, and cytostatic). These activities are mainly attributed to the presence of flavonoids in propolis, which points out the interest in quantifying these constituents in propolis preparations, as well as validation of analytical methodologies. High-performance liquid chromatography (HPLC) methods have been reported to quantify isolated flavonoids or these compounds in complex biological matrices, such as herbal raw materials and extractive preparations. An efficient, precise, and reliable method was developed for quantification of propolis extractive solution using HPLC with UV detection. The chromatograms were obtained from various gradient elution systems (GES) tested in order to establish the ideal conditions for the analysis of propolis extractive solution, using methanol and water: acetonitrile (97.5 : 2.5, v/v) as mobile phase. Gradient reversed phase chromatography was performed using a stainless steel column (250 x 4.6 mm i.d., 5 mum) filled with Chromsep RP 18 (Varian), column temperature at 30.0 +/- 0.1degreesC and detection at 310 nm. The main validation parameters of the method were also determined. The method showed linearity for chrysin in the range 0.24-2.4 mug mL(-1) with good correlation coefficients (0.9975). Precision and accuracy were determined. The obtained results demonstrate the efficiency of the proposed method. The analytical procedure is reliable and offers advantages in terms of speed and cost of reagents.en
dc.description.affiliationUNESP, Programa Posgraduacao Ciências Farmaceut, BR-14802902 Araraquara, SP, Brazil
dc.description.affiliationUnespUNESP, Programa Posgraduacao Ciências Farmaceut, BR-14802902 Araraquara, SP, Brazil
dc.format.extent2399-2409
dc.identifierhttp://dx.doi.org/10.1081/JLC-120023254
dc.identifier.citationJournal of Liquid Chromatography & Related Technologies. New York: Marcel Dekker Inc., v. 26, n. 14, p. 2399-2409, 2003.
dc.identifier.doi10.1081/JLC-120023254
dc.identifier.issn1082-6076
dc.identifier.urihttp://hdl.handle.net/11449/7549
dc.identifier.wosWOS:000184983400012
dc.language.isoeng
dc.publisherMarcel Dekker Inc
dc.relation.ispartofJournal of Liquid Chromatography & Related Technologies
dc.relation.ispartofjcr0.827
dc.relation.ispartofsjr0,297
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectpropolispt
dc.subjecthigh-performance liquid chromatography (HPLC)pt
dc.subjectchrysinpt
dc.subjectphytochemicalspt
dc.subjectflavonoidspt
dc.titleApplication of an HPLC method for analysis of propolis extracten
dc.typeArtigopt
dcterms.licensehttp://journalauthors.tandf.co.uk/permissions/reusingOwnWork.asp
dcterms.rightsHolderMarcel Dekker Inc
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentFármacos e Medicamentos - FCFpt

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